510(k) K112700 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
FRONTIER SADL INTERBODY FUSION DEVICE
| Applicant | Frontier Medical Devices, Inc., Apple Valley MN, US |
| Decision | Substantially Equivalent, Nov 1, 2012 |
| Received | Sep 16, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112700
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.